chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X4697896546978966GT39GENIChomozygous108257570
X4699027846990279GT22GENIChomozygous108732008
X4699037246990373GT62GENICpossibly homozygous119918744
X4699041646990417TG64GENIChomozygous119918745
X4699952746999528TA53GENICheterozygous119997262
X4699953346999534AT54GENICheterozygous119997264
X4700349947003500TA13GENIChomozygous119997265
X4700354147003542TA28GENIChomozygous119918750
X4700358147003582CT25GENIChomozygous119918751
X4700361047003611GT14GENIChomozygous119997267
X4700365247003653CA22GENIChomozygous119918752
X4700380447003805CA13GENIChomozygous119997269
X4701675447016755TA68GENIChomozygous108257576